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Spinal anesthesia using hyperbaric levobupivacaine and ropivacaine

Evaluation of 0.5% hyperbaric levobupivacaine and 0.75% hyperbaric ropivacaine for elective infraumblical surgeries under spinal anaesthesia - A comparative study - NIL

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/12/060908
Enrollment
80
Registered
2023-12-28
Start date
Unknown
Completion date
Unknown
Last updated
2024-01-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: O- Medical and Surgical

Interventions

Intervention1: 0.75% hyperbaric ropivacaine 22.5mg stat intrathecal: To compare the onset and duration of sensory and motor blockade, maximum level of sensory blockade and hemodynamic parameters for 3

Sponsors

Dr Soma Sundaram A
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients of American society of Anaesthesiologists physical status classification I and II Infraumblical surgeries Elective surgeries Age 18-65 years BMI less than 30 Patient who have given valid informed written consent.

Exclusion criteria

Exclusion criteria: Patients of American society of Anaesthesiologists physical status classification III and IV Emergency surgeries Patient refusal Local Infection Coagulopathy Spine deformity Pregnancy Allergy to study drugs Change in plan of anaesthesia during introperative period

Design outcomes

Primary

MeasureTime frame
To compare the onset & duration of sensory and motor blockade & maximum level of sensory blockade & time to achieve itTimepoint: sensory & motor blockade tested at 1 min interval for the first 5 min after the spinal injection subsequently at 3min interval in the next half an hour and every 15 min interval till the completion of surgical procedure

Secondary

MeasureTime frame
To determine the hemodynamic parameters & incidence of any complications side effectsTimepoint: Vital parameters will be recorded at 1 3 5 10 15 30 45 60 75 90 120 mins after subarachnoid blockade

Countries

India

Contacts

Public ContactDr Soma Sundaram A

Sri Muthukumaran medical college hospital and research institute

drrvanaes@gmail.com9444066434

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026